Evidence map›Paper›PMID 27547713›Full record

ArticleCurrent stem cell reports2016

MicroRNAs in Control of Stem Cells in Normal and Malignant Hematopoiesis.

Christine Roden, Jun Lu

Open access · bronzeAbstract read
In one paragraph

Article in Current stem cell reports, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
1.2field-weighted citation impact, top 23% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

15 citing papers in PubMed, 22 citations in OpenAlex.

  1. Article
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  8. Article
  9. Identification of osteolineage cell-derived extracellular vesicle cargo implicated in hematopoietic support.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2020
    Article
  10. Review
  11. Article
  12. Review
  13. Blood · 2017
    Article
  14. Article
  15. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

2 authors at 1 institution in 1 country.

Christine RodenDepartment of Genetics, Yale University School of Medicine, New Haven, Connecticut 06510, USA; Yale Stem Cell Center, Yale Cancer Center, New Haven, Connecticut, 06520, USA; Graduate Program in Biological and Biomedical Sciences, Yale University, New Haven, Connecticut 06510, USA.
Jun LuDepartment of Genetics, Yale University School of Medicine, New Haven, Connecticut 06510, USA; Yale Stem Cell Center, Yale Cancer Center, New Haven, Connecticut, 06520, USA; Yale Center for RNA Science and Medicine, New Haven, Connecticut, 06520, USA.
Yale University · US

Funding

GENETICS AND GENOMICS OF HUMAN DISEASET32HD007149 · NICHD · YALE UNIVERSITY · PI James P Noonan · 1985 to 2026
$8.2M
Novel Approaches to Mammalian MicroRNA Target PredictionR01GM099811 · NIGMS · WADSWORTH CENTER · PI DING, YE, LU, JUN · 2012 to 2015
$2.4M
Quantitative Modeling of MicroRNA:Target Interactions in Cell Fate TransitionR01GM116855 · NIGMS · WADSWORTH CENTER · PI DING, YE, LU, JUN · 2016 to 2019
$2.2M
The role of microRNAs in leukemic initiation and maintenanceR01CA149109 · NCI · YALE UNIVERSITY · PI LU, JUN · 2011 to 2015
$1.7M
NCI NIH HHS R01 CA149109NICHD NIH HHS T32 HD007149NIGMS NIH HHS R01 GM099811NIGMS NIH HHS R01 GM116855
6 · The paper itself

Abstract

Studies on hematopoietic stem cells (HSCs) and leukemia stem cells (LSCs) have helped to establish the paradigms of normal and cancer stem cell concepts. For both HSCs and LSCs, specific gene expression programs endowed by their epigenome functionally distinguish them from their differentiated progenies. MicroRNAs (miRNAs), as a class of small non-coding RNAs, act to control post-transcriptional gene expression. Research in the past decade has yielded exciting findings elucidating the roles of miRNAs in control of multiple facets of HSC and LSC biology. Here we review recent progresses on the functions of miRNAs in HSC emergence during development, HSC switch from a fetal/neonatal program to an adult program, HSC self-renewal and quiescence, HSC aging, HSC niche, and malignant stem cells. While multiple different miRNAs regulate a diverse array of targets, two common themes emerge in HSC and LSC biology: miRNA mediated regulation of epigenetic machinery and cell signaling pathways. In addition, we propose that miRNAs themselves behave like epigenetic regulators, as they possess key biochemical and biological properties that can provide both stability and alterability to the epigenetic program. Overall, the studies of miRNAs in stem cells in the hematologic contexts not only provide key understandings to post-transcriptional gene regulation mechanisms in HSCs and LSCs, but also will lend key insights for other stem cell fields.

Indexed as

epigenetic machineryhematopoietic stem cellsleukemia stem cellsmiRNAs

Identifiers

PMID27547713
PMCPMC4988405
OpenAlexW2464674049

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.